A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059124



Internal ID18801655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..33908301hg38UCSC Ensembl
Innerchr16:32058483..33710768hg19UCSC Ensembl
Innerchr16:31965984..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381861140
hg191652286
hg181652286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3549281, nssv3549282
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059124
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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